Medicarpin
CAS No. 32383-76-9
Medicarpin ( —— )
产品货号. M21689 CAS No. 32383-76-9
Medicarpin a legume phytoalexin acts as an estrogen receptor (ER) agonist can stimulate osteoblast differentiation likely via ERα2 promote achievement of peak bone mass and is devoid of uterine estrogenicity; in addition given its excellent oral bioavailability it can be potential osteogenic agent.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥3208 | 有现货 |
|
10MG | ¥4293 | 有现货 |
|
25MG | ¥6958 | 有现货 |
|
50MG | ¥9558 | 有现货 |
|
100MG | ¥12879 | 有现货 |
|
200MG | 获取报价 | 有现货 |
|
500MG | 获取报价 | 有现货 |
|
1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Medicarpin
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述Medicarpin a legume phytoalexin acts as an estrogen receptor (ER) agonist can stimulate osteoblast differentiation likely via ERα2 promote achievement of peak bone mass and is devoid of uterine estrogenicity; in addition given its excellent oral bioavailability it can be potential osteogenic agent.
-
产品描述Medicarpin a legume phytoalexin acts as an estrogen receptor (ER) agonist can stimulate osteoblast differentiation likely via ERα2 promote achievement of peak bone mass and is devoid of uterine estrogenicity; in addition given its excellent oral bioavailability it can be potential osteogenic agent.
-
同义词——
-
通路Immunology/Inflammation
-
靶点ROS
-
受体ROS;JNK;Bcl-2
-
研究领域——
-
适应症——
化学信息
-
CAS Number32383-76-9
-
分子量270.3
-
分子式C16H14O4
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESCOc1cc(O[C@H]2c(ccc(O)c3)c3OC[C@@H]22)c2cc1
-
化学全称(6aS11aS)-9-methoxy-6a11a-dihydro-6H-benzofuro[32-c]chromen-3-ol
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Effect of lead treatment on medicarpin accumulation and on the gene expression of key enzymes involved in medicarpin biosynthesis in Medicago sativa L.Environ Sci Pollut Res Int. 2014 Dec;21(24):14091-8.
产品手册
关联产品
-
F-1
?F-1 is IC50s of 2.1 nM, 2.3 nM, 1.3 nM and 3.9 nM for ALKWT, ROS1WT, ALKL1196M and ALKG1202R, respectively.?F-1 is a potent ALK and ROS1 dual inhibitor, suppresses phospho-ALK and its relative downstream signaling pathways.
-
Topiroxostat
Topiroxostat(FYX-051) is a novel and potent xanthine oxidoreductase (XOR) inhibitor with IC50 value of 5.3 nM.
-
Daidzin 6''-O-malona...
Daidzin 6''-O-malonate may have anticancer activity.